Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008723 0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10192157 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10206753 1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs1043828 1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs11078925 0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11078927 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs11557466 0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 3
rs11557467 0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs11870965 0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs12603332 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 3
rs12936231 0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs12950743 0.925 0.160 17 39892980 intergenic variant T/C snv 0.45 3
rs13408569 1.000 0.080 2 102338596 intron variant G/C snv 0.18 2
rs13408661 1.000 0.080 2 102338622 intron variant G/A snv 0.18 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs13431828 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2
rs1362348 1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7